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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs632639          
refSNP ID: rs632639
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:83/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/T
Ancestral Allele:C
Clinical Association:unknown
HGVS Names
NM_032807.3:c.907-117A>G
NM_178150.1:c.754-117A>G
NT_077569.2:g.313667A>G
Links

SNP Details are organized in the following sections:
Submission Fasta Resource GeneView Map Diversity Validation

  Submitter records for this RefSNP Cluster back to top
The submission ss10640436 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs632639 during BLAST analysis for the current build.

NCBI
Assay ID
Handle|Submitter IDValidation
Status
ss to rs
Orientation
/Strand
Alleles5' Near Seq 30 bp3' Near Seq 30 bpEntry
Date
Update
Date
Build
Added
Molecule
Type
Freq
Warning
Ancestral
Allele
Success
Rate
ss805253SC_JCM|AL137186.5_41710rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct07/27/0010/10/0383Genomicunknown
ss971003KWOK|OVLP-000804-516620fwd/BC/Taggagtttgagactagcatggccaacatgggaagccccgtctctactgaaaaaaaataca09/01/0010/10/0386Genomic99 %
ss1868154KWOK|OVLP-000925-66147fwd/BC/Taggagtttgagactagcatggccaacatgggaagccccgtctctactgaaaaaaaataca10/06/0010/10/0387Genomic99 %
ss3063390TSC-CSHL|TSC1152175fwd/BC/Taggagtttgagactagcatggccaacatgggaagccccgtctctactgaaaaaaaataca06/07/0110/10/0396Genomicunknown
ss3899610SC_JCM|AL137186.11_154279fwd/BC/Taggagtttgagactagcatggccaacatgggaagccccgtctctactgaaaaaaaataca09/25/0110/10/03100Genomicunknown
ss10640436BCM_SSAHASNP|chr10.NT_077569.2_313667rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct06/29/0310/10/03116Genomicunknown
ss16007742SC_SNP|NT_077569.2_313667rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct11/18/0311/22/03120Genomicunknown
ss16508797CSHL-HAPMAP|CSHL-HuAA-200402.chr10.NT_077569.2_313667rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct02/17/0403/04/04120Genomicunknown
ss17410513CSHL-HAPMAP|CSHL-HuCC-200402.chr10.NT_077569.2_313667rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct02/19/0403/04/04120Genomicunknown
ss19188740CSHL-HAPMAP|CSHL-HuDD-200402.chr10.NT_077569.2_313667rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct02/20/0403/04/04120Genomicunknown
ss20717120SSAHASNP|WGSA-200403-chr10.chr10.NT_077569.2_313667rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct03/18/0403/19/04121Genomicunknown
ss39784840ABI|hCV921090rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct07/16/0507/16/05126Genomicunknown
ss88079637BCMHGSC_JDW|JWB-0228867rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct02/26/0802/27/08129Genomicunknown
ss1091945681000GENOMES|CEU.trio.12.15.2008_2285597_chr10_5990777rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct12/15/0812/16/08130Genomicunknown
ss1153005461000GENOMES|NA19240_2008_12_16_2064996_chr10_5990777rev/TA/Gtgtattttttttcagtagagacggggcttcccatgttggccatgctagtctcaaactcct12/18/0812/19/08130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs632639|allelePos=255|totalLen=2155|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=130
 AGCTCACCGT ATGAGGTTCA GCACACACAG GTCTGACTCC TTTTCTATGC CACAGTTAGA
 CAGGATGCCG TCCACTTTGC TGACAGCTTG CTCTTCATTC ATCAGGTATC GATGGTACAG
 CTTCTTCCAA GGAATGAACT ATGCAGTTAA AAAACAAACA AAATAACATG AGGCAAAGGG
 CCATTAGAAA GCAGATTAAT gaggcgggca gatcgcctga ggtcaggagt ttgagactag
 catggccaac atgg
 Y
 gaagccccgt ctctactgaa aaaaaataca aaaattagcc aggcatgatg gcacatgcct
 gtagtcccag ctactcagga agctgaggca ggagaatcac ttgaacctgg gaggcggagg
 ttgcagtgag ccgagatcaa gccactgcag tgcacgctag cctgggtgac agagtgagac
 tccatctcaa aaaaaaaaaa agaaagaaaa aaaGCAGATT AAGCCACAAA CACATAGATA
 ACCTTTTACC AGTGAAAAGC AATCACAGCT CACAATTCAA AAGCCAGGAA AATCAGGCAG
 AAATGTTACA CAAATTTTTG TTGGAAACTA GGAGAACTGG GTCTTGGTCT TGGTTCTAAC
 ActaACTTGT TATAGTTAAA GAATCTGGGA AAAACTATAG CTTCAGTTTC CCTGTCTGAA
 ACATTAGTAC ACGTAACTCA GGGTTTCAat gggaacaaaa taatatgaga gctgtggcta
 tactaatatc agacaaaaca gactttaagt caattctgtc tgttaaatac tgttataaga
 gacgaaggac ataatgataa aagggtcaat tcaccaagaa gatataataa ctataaatat
 atatgcacca cacattagag ctcctaaata taggaaacaa cccctgacag aactgaaggt
 agaaaccaac agcaacacaa taatagaagg agatttcaac actgctattt caatgatgga
 tggaacaacc agacagaaga taaataagga aaacagagga tctgaacaac actatggact
 aagcgggctg aacgaacata tacagaatac tccacccaac aacagcaaaa tatacattcc
 tctcaagggc acatgaaaca ttctccagga tagatcacct gttaggccac aaaacaagtt
 tcaacaaact taaaaaccac ttaagttatt atatgaagta tctttttaaa tcacaatgga
 atgtaaccag aaatcaatag cagaaggaaa actgaaaaat ccacaaatat atggatatta
 aacaacatac ccttgcccag gcacagtggt ttatgcctgt aatccctgca ctttgggcag
 ctgagacagg cggatcactt aaggccagga ctttgagacc atcctggatt acatggtgaa
 accctatctc tcctaaaaat acaaaaatta gccaggcatg gtggcacatg tctgtaatcc
 cagctacttg ggaggctaag gcacaagaat cacttgaact tgggaggtgg aggttgcagt
 gagccaaagt cgagccactg cactccagcc tgggtgacag agcaagactc tgtctcaaaa
 aaaaaaaaaa aaaaaccaac aacaacaaaa aacacattct taaaacaacc aatgggtcaa
 agaagaaatc acaaagaaaa gtagaaaata tcttgagaca aatgaaaatg aaaacataac
 ataccaaaac ttatgaaatg caatgaatgc tgttgggctg ttttaagaga ggggtttatt
 gctataaatg cttacactca aacaaacaaa caaacaaaAA ATGggccaga catggtggct
 cacgcctgta accccagcac ttgggaggct gatggcaggc agatcacttg aagttaggag
 tttcagagac catcctggcc aacatggtaa aaccccatgt ctactgaaaa tacaaaaatt
 agccgggtgt ggtggcgcac gcctgtaatc ccagctactg gggaggctga ggcaggagaa
 tcacttgaac ctgggaggca gaggttgcag tgagtcagga tcgtgccact gcactccagc
 ctgggcaaca gtgggaaact ctgtctcaaa aaaaaaaaaa aagaaGTCAA GGGAGATATG
 AGGAACCCTC CAGGTGGGGA AGGTGGGAGG ATGAGAGCAA

  GeneView back to top
GeneView via analysis of contig annotation: FBXO18 F-box protein, helicase, 18
View variations for gene:
Include clinically associated: in gene region cSNP has frequency double hit
Group
Label
Contig->mRNAGene Model (contig mRNA transcript) Color Legend
referenceNT_077569->NM_032807
svfunction
referenceNT_077569->NM_178150
svfunction
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_077569->NM_032807->NP_116196313667forwardintron
referenceNT_077569->NM_178150->NP_835363313667forwardintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs632639 maps exactly once on NCBI human chromosome 10
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
10NW_001837931.2249044065877571plusCalt_assembly_8HuRefHuRefview254
10NW_924584.158811645881164minusGalt_assembly_1CeleraCeleraview254
10NT_077569.23136675990777minusAref_assemblyreferencereferenceview254

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_077569 AC053504 AL137186.5 AL137186.6
dbSNP Blast Analysis
GenBank HTGS Finished:
AL137186.18

  Population Diversity back to top
There is no frequency data.

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterwith2hit
DoubleHit found by:  BCM_SSAHASNPNCBI
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .